Canonical Allele Identifier: CA407041305

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411855C>T (hg19) ; chr19:g.50908599C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908599C>T , CM000681.2:g.50908599C>T	GRCh38
NC_000019.9:g.51411855C>T , CM000681.1:g.51411855C>T	GRCh37
NC_000019.8:g.56103667C>T	NCBI36
NG_012154.2:g.7140G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324041.6:c.455G>A MANE Select	ENSP00000326159.1:p.Gly152Asp
ENST00000324041.5:c.455G>A	ENSP00000326159.1:p.Gly152Asp
ENST00000431178.2:c.308G>A	ENSP00000399448.2:p.Gly103Asp
ENST00000593885.1:c.170G>A	ENSP00000469769.1:p.Gly57Asp
ENST00000596876.1:n.374G>A
ENST00000598305.5:c.170G>A	ENSP00000469963.1:p.Gly57Asp
ENST00000599865.5:n.308G>A
ENST00000602148.1:c.467G>A	ENSP00000472091.1:n.467G>A
NM_001302961.1:c.170G>A	NP_001289890.1:p.Gly57Asp
NM_004917.4:c.455G>A	NP_004908.4:p.Gly152Asp
NR_126566.1:n.448G>A
XM_005259441.3:c.170G>A	XP_005259498.2:p.Gly57Asp
XM_011527545.1:c.455G>A	XP_011525847.1:p.Gly152Asp
XM_011527546.1:c.455G>A	XP_011525848.1:p.Gly152Asp
XM_011527547.1:c.308G>A	XP_011525849.1:p.Gly103Asp
XM_005259441.4:c.170G>A	XP_005259498.2:p.Gly57Asp
XM_011527545.3:c.455G>A	XP_011525847.1:p.Gly152Asp
XM_011527546.2:c.455G>A	XP_011525848.1:p.Gly152Asp
NM_001302961.2:c.170G>A	NP_001289890.1:p.Gly57Asp
NR_126566.2:n.448G>A
NM_004917.5:c.455G>A MANE Select	NP_004908.4:p.Gly152Asp